Godelieve Morel
6PUBLICATIONS
124CO-AUTHORS
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Publications (6)
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|Mar 30, 2026
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies.Elsa Leitão, Amandine Santini, Benjamin Cogne
|Mar 26, 2026
DNA methylation signature and clinical delineation of PACS1-related disorder in 24 unreported individuals.Quentin Sabbagh, Camille Cenni, Sadegheh Haghshenas
|Aug 29, 2024
First Description of a Large Clinical Series of Fetal Alcohol Spectrum Disorders Children and Adolescents in Reunion Island, France.Laëtitia Sennsfelder, Susie Guilly, Sonia Henkous
|Oct 23, 2023
Episignatures in practice: independent evaluation of published episignatures for the molecular diagnostics of ten neurodevelopmental disorders.Thomas Husson, François Lecoquierre, Gaël Nicolas
|Dec 02, 2022
Correction to: Evaluation of somatic and/or germline mosaicism in congenital malformation of the eye.Bertrand Chesneau, Véronique Ivashchenko, Christophe Habib
|Nov 20, 2022
Evaluation of somatic and/or germline mosaicism in congenital malformation of the eye.Bertrand Chesneau, Véronique Ivashchenko, Christophe Habib
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Frequent Collaborators
3 joint publications
Bertrand Chesneau
3 joint publications
Julien Van-Gils
3 joint publications
Marlène Rio
3 joint publications
Gaëtan Lesca
3 joint publications
Massimiliano Rossi
3 joint publications
Nicolas Chatron
2 joint publications
Christophe Habib
2 joint publications
Véronique Gaston
2 joint publications
Julie Plaisancié
2 joint publications
Gaël Nicolas
